BONE GRAFT WASHER

GUDID 00673978958934

WASHER 9090117 TI BONE GRAFT 17MM

MEDTRONIC SOFAMOR DANEK, INC.

Bone-screw internal spinal fixation system, non-sterile
Primary Device ID00673978958934
NIH Device Record Keya8a27263-1d5f-40d9-9c86-961c39a32da9
Commercial Distribution StatusIn Commercial Distribution
Brand NameBONE GRAFT WASHER
Version Model Number9090117
Company DUNS830350380
Company NameMEDTRONIC SOFAMOR DANEK, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com
Phone+1(800)633-8766
EmailCorporate.UDI@medtronic.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100673978958934 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWQAPPLIANCE, FIXATION, SPINAL INTERVERTEBRAL BODY

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00673978958934]

Moist Heat or Steam Sterilization


[00673978958934]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-08-05

On-Brand Devices [BONE GRAFT WASHER]

00613994543578WASHER X050710319 19MM CLOVER
00673978958934WASHER 9090117 TI BONE GRAFT 17MM
00673978958910WASHER 9090115 TI BONE GRAFT 15MM

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